一种简单而灵敏的念珠菌定植、监测和感染控制检测方法,适合患者就近使用。

IF 6.1 2区 医学 Q1 MICROBIOLOGY Journal of Clinical Microbiology Pub Date : 2024-07-16 Epub Date: 2024-06-18 DOI:10.1128/jcm.00525-24
Sukalyani Banik, Burcu Ozay, Marisol Trejo, YanChun Zhu, Charan Kanna, Cynthia Santellan, Bennett Shaw, Sukantha Chandrasekaran, Sudha Chaturvedi, Lindy Vejar, Soumitesh Chakravorty, David Alland, Padmapriya Banada
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引用次数: 0

摘要

念珠菌是一种具有多种耐药性的真菌病原体,具有在人体定植和在环境表面持久存在的倾向。在急诊和长期护理环境中发现的念珠菌侵袭性真菌病越来越多。我们已开发出一种基于盒式检测器的C. auris监测原型(CaurisSurV盒式检测器;"仅供研究使用"),该检测器集成了样本处理和核酸扩增功能,可在GeneXpert仪器中检测监测皮肤拭子中的C. auris,专为护理点使用而设计。皮肤拭子基质中的非聚集菌株(AR0388)和聚集菌株(AR0382)的检测限(LoD)分别为 10.5 CFU/mL 和 14.8 CFU/mL。在 LoD 为 2-3-5 倍(31.5-52.5 CFU/mL)时,可检测到所有五个已知的弓形虫支系。该检测方法通过两个不同机构(加州大学洛杉矶分校和纽约州沃兹沃思中心)的 85 份临床拭子样本库进行了验证。与培养相比,加州大学洛杉矶分校和沃兹沃思中心的灵敏度分别为 96.8%(30/31)和 100%(10/10),综合灵敏度为 97.5%(40/41);与 PCR 相比,综合灵敏度为 92%(46/50)。对临床样本(阴性阴沟球菌基质,N = 31)和分析样本(非阴沟球菌菌株,N = 32)的特异性均为 100%。对纽约州沃兹沃思中心的 N = 60 份样本进行的另一项盲法研究显示,灵敏度为 97%(29/30),特异性为 100%(28/28)。我们开发出了一种完全集成、灵敏、特异且只需 58 分钟的原型检测方法,可用于对阿氏杆菌的常规监测,并有助于预防急性和慢性医疗机构中的定植和疫情爆发:本研究有可能为医院和长期护理机构的医护人员提供更好的解决方案,帮助他们及时有效地控制念珠菌感染,从而更快地应对未来可能爆发的疫情。
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A simple and sensitive test for Candida auris colonization, surveillance, and infection control suitable for near patient use.

Candida auris is a multidrug-resistant fungal pathogen with a propensity to colonize humans and persist on environmental surfaces. C. auris invasive fungal disease is being increasingly identified in acute and long-term care settings. We have developed a prototype cartridge-based C. auris surveillance assay (CaurisSurV cartridge; "research use only") that includes integrated sample processing and nucleic acid amplification to detect C. auris from surveillance skin swabs in the GeneXpert instrument and is designed for point-of-care use. The assay limit of detection (LoD) in the skin swab matrix was 10.5 and 14.8 CFU/mL for non-aggregative (AR0388) and aggregative (AR0382) strains of C. auris, respectively. All five known clades of C. auris were detected at 2-3-5× (31.5-52.5 CFU/mL) the LoD. The assay was validated using a total of 85 clinical swab samples banked at two different institutions (University of California Los Angeles, CA and Wadsworth Center, NY). Compared to culture, sensitivity was 96.8% (30/31) and 100% (10/10) in the UCLA and Wadsworth cohorts, respectively, providing a combined sensitivity of 97.5% (40/41), and compared to PCR, the combined sensitivity was 92% (46/50). Specificity was 100% with both clinical (C. auris negative matrix, N = 31) and analytical (non-C. auris strains, N = 32) samples. An additional blinded study with N = 60 samples from Wadsworth Center, NY yielded 97% (29/30) sensitivity and 100% (28/28) specificity. We have developed a completely integrated, sensitive, specific, and 58-min prototype test, which can be used for routine surveillance of C. auris and might help prevent colonization and outbreaks in acute and chronic healthcare settings.

Importance: This study has the potential to offer a better solution to healthcare providers at hospitals and long-term care facilities in their ongoing efforts for effective and timely control of Candida auris infection and hence quicker response for any potential future outbreaks.

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来源期刊
Journal of Clinical Microbiology
Journal of Clinical Microbiology 医学-微生物学
CiteScore
17.10
自引率
4.30%
发文量
347
审稿时长
3 months
期刊介绍: The Journal of Clinical Microbiology® disseminates the latest research concerning the laboratory diagnosis of human and animal infections, along with the laboratory's role in epidemiology and the management of infectious diseases.
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